Phosphine, tris(3,5-dimethylphenyl)-
Grundinformationen
- CAS
69227-47-0- Standard-SMILES
Cc1cc(C)cc(P(c2cc(C)cc(C)c2)c2cc(C)cc(C)c2)c1- InChIKey
XRALRSQLQXKXKP-UHFFFAOYSA-N- Summenformel
- C24H27P
- Durchschnittliche Molmasse
- 346,4 g/mol
- Monoisotopische Masse
- 346,18503786
Namen und Bezeichner
- Bevorzugter Name
- Phosphine, tris(3,5-dimethylphenyl)-
- IUPAC
- tris(3,5-dimethylphenyl)phosphane
- Englischer Name
- Tris(3,5-dimethylphenyl)phosphine
- Summenformel
- C24H27P
- Molmasse
- 346.44
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
69227-47-0- PubChem CID
- 112263
- DTXSID
DTXSID5071969- EC Number
- 624-162-2
- Nikkaji
- J38.110A
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 6,8
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 0
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 25
- Formalladung
- 0
- Komplexität
- 327
Physikochemische Eigenschaften
- Schmelzpunkt
- 160 · 160-165 °C
- Siedepunkt
- 474.1 · 474.1±45.0 °C(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- Aggregatzustand
- crystal
- Farbe
- white
- InChI
- 1S/C24H27P/c1-16-7-17(2)11-22(10-16)25(23-12-18(3)8-19(4)13-23)24-14-20(5)9-21(6)15-24/h7-15H,1-6H3
- InChIKey
- XRALRSQLQXKXKP-UHFFFAOYSA-N
- SMILES
- Cc1cc(C)cc(c1)P(c2cc(C)cc(C)c2)c3cc(C)cc(C)c3
- EPA chemische Informationen
- Phosphine, tris(3,5-dimethylphenyl)- (69227-47-0)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 40 reports by companies from 2 notifications to the ECHA C&L Inventory.
Gefahrenhinweise
Sicherheitsdaten
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 29310099
- risk_code
- 22
- hazard_code
- Xn
- safety_code
- 26-36/37/39-22
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Acute Tox. 4 Oral
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
VerwendenCatalyst for:Cu / diphosphine-catalyzed asymmetric hydrogenation of heteroaromatic ketones and enonesHighly selective rhodium-catalyzed hydrogenation reactionsClassical versus kinetic resolution in preparation of privileged silicon-stereogenic silanaphthalenesUsed for kinetic resolution of donor-functionalized secondary alcohols via Cu-H-catalyzed stereoselective silylation by dehydrogenative Si-O coupling with Si-stereogenic silanesUsed for comparative studies of conformational rigidity of silicon-stereogenic silanes in asymmetric catalysis
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